Canonical Allele Identifier: CA572795697
Gene: UMAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1184111068
gnomAD v2: 7-7848975-A-G
gnomAD v3: 7-7809344-A-G
gnomAD v4: 7-7809344-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7809344A>G , CM000669.2:g.7809344A>G GRCh38
NC_000007.13:g.7848975A>G , CM000669.1:g.7848975A>G GRCh37
NC_000007.12:g.7815500A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000682710.1:c.156+7601A>G MANE Select ENSP00000507605.1:n.156+7601A>G
ENST00000406829.2:n.168+7601A>G
ENST00000463725.5:n.396+7601A>G
ENST00000482067.3:n.247+7601A>G
ENST00000636849.1:c.156+7601A>G ENSP00000489648.1:n.156+7601A>G
ENST00000638342.1:c.156+7601A>G ENSP00000491286.1:n.156+7601A>G
ENST00000639110.1:c.156+7601A>G ENSP00000491319.1:n.156+7601A>G
ENST00000639343.1:c.*58+7601A>G ENSP00000491077.1:n.*58+7601A>G
NM_001302348.1:c.156+7601A>G NP_001289277.1:n.156+7601A>G
NM_001302349.1:c.156+7601A>G NP_001289278.1:n.156+7601A>G
NM_001302350.1:c.51+7601A>G NP_001289279.1:n.51+7601A>G
NM_001302348.2:c.156+7601A>G MANE Select NP_001289277.1:n.156+7601A>G
NM_001302349.2:c.156+7601A>G NP_001289278.1:n.156+7601A>G
NM_001302350.2:c.51+7601A>G NP_001289279.1:n.51+7601A>G